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CompletedNCT04666012Updated Jul 28, 2023

Safety and Immunogenicity Study of AdCLD-CoV19: A COVID-19 Preventive Vaccine in Healthy Volunteers

A Phase 1/2 interventional study of AdCLD-CoV19 in COVID-19, sponsored by Cellid Co., Ltd.. Completed at 5 sites in Korea, Republic of. Open to participants aged 19 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-07-28.

Sponsored by Cellid Co., Ltd. · Phase 1/2, Interventional, and Prevention

Phase
Phase 1/2
Study type
Interventional
Enrollment
150
Allocation
Non-randomized
Ages
19 Years to 64 Years
Sex
All
01

Study summary

This is a Phase 1/2a clinical trial to assess the safety and immunogenicity of AdCLD-CoV19 in healthy adults.

Read the detailed description

Part A is conducted as dose-escalation, single-center, open-label, a Phase 1 clinical trial. Part B is conducted as multi-center, open-label, a Phase 2a clinical trial. In Part A, we assess safety in all dose groups and set suitable two doses for Part B. In Part B, we assess immune responses against SARS-CoV-2 and set suitable dose for next phase of clinical trial. DSMB will evaluate safety during the whole study period.

02

Conditions studied

  • COVID-19

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03

In context

COVID-19

7,638 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 150 is above the median of 100 across 4,098 interventional studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

Cellid Co., Ltd. is the lead sponsor of 8 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Able and willing to agree informed consent and aged 19 to 64 years.
  2. The BMI index is 18.5 kg/m2 to 30.0 kg/m2.
  3. Weigh 40kg to 100kg (Part A only)
  4. Able and willing to medically effective contraception during the whole study period.
  5. Agreement to refrain from blood donation during the whole study period.

Exclusion criteria

Exclusion Criteria:

  1. Anyone deemed infected by COVID-19.
  2. Determined to be a close-contact of SARS-CoV-2 confirmed case or classified to symptomatic patient of COVID-19 prior to vaccination.
  3. Clinically significant abnormal ranges of laboratory measurement, ECG, Chest X-ray at screening visit.
  4. Positive in HIV, HBV, HCV test at screening visit.
  5. Acute fever(≥ 38℃) or suspected infectious disease, symptoms of infectious disease(cough, difficulty breathing, chills, muscle aches, headache, sore throat, loss of smell, or loss of taste, etc.) within 3 days prior to vaccination.
  6. Chronic respiratory disease: Asthma, chronic obstructive pulmonary disease, active tuberculosis, latent tuberculosis under treatment.
  7. Clinically significant active or any history of disease: Hepatobiliary system, kidney, central or peripheral nervous system (epilepsy, seizure, etc.), endocrine system (uncontrolled diabetes, hyperlipidemia, etc.), cardiovascular system (congestive heart failure, coronary artery disease, myocardial infarction, control Hypertension, etc.), blood tumor, urinary system, mental, musculoskeletal system, immune system (rheumatoid arthritis, systemic lupus erythematosus).
  8. Immunosuppressive disease including immunodeficiency disease.
  9. Scheduled to undergo any surgery during the whole study period.
  10. Healthcare worker who provide medical care to SARS-CoV-2 cases or occupationally in high risk for SARS-CoV-2 exposure during the whole study period.
  11. Prisoners or subjects who are compulsorily detained. (involuntary incarceration)
  12. History of SARS or MERS.
  13. Allergic reaction or hypersensitivity to any ingredient of AdCLD-CoV19.
  14. Having hemophilia at risk of causing serious bleeding when injected intramuscularly or receiving anticoagulants.
  15. Any history of malignant disease within the past 5 years.
  16. History of hypersensitivity to inoculate vaccine such as Guillain-Barre syndrome.
  17. History of serious adverse reaction or allergic reaction to inoculate vaccine.
  18. Urticaria past 5 years prior to vaccination.
  19. History of hereditary angioneurotic edema or acquired angioneurotic edema.
  20. History of solid organ or bone marrow transplantation.
  21. Suspected or a history of drug or alcohol abuse past 12 month before vaccination.
  22. Receipt of vaccine of SARS-CoV, MERS-CoV, SARS-CoV-2.
  23. Receipt of adenovirus vector based vaccine.
  24. Chronic use of immunosuppressant or immune modifying drug within 6 months prior to vaccination. (use of inhaled, topical, nasal, and ophthalmic corticosteroids are allowed)
  25. Having relied on antipsychotic drugs and narcotic analgesics within 6 months before vaccination or difficult to comply with the clinical trial procedure at the judgment of the investigator.
  26. Administered to other investigational product or medical device within 6 months before vaccination.
  27. Other vaccination history within 30 days prior to vaccination or being scheduled within 30 days after vaccination.
  28. Receipt of immunoglobulin or any blood product within 3 month prior to vaccination.
  29. Pregnant(including positive hCG test at screening visit) or breastfeeding female.
  30. Current smoker or vaper. (use of cigarette or e-cigarette at least once in last 30 days, Part A only)
  31. Those who are directly related to the investigator.
  32. Other condition deemed ineligible for the study at the discretion of investigator.
05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
150 participants (actual)

Study arms

  • Experimental
    Group 1: low dose

    Subject will receive single dose of AdCLD-CoV19(2.5x10\^10VP) as intramuscular injection.

    Biological: AdCLD-CoV19

  • Experimental
    Group 2: middle dose

    Subject will receive single dose of AdCLD-CoV19(5.0x10\^10VP) as intramuscular injection.

    Biological: AdCLD-CoV19

  • Experimental
    Group 3: high dose

    Subject will receive single dose of AdCLD-CoV19(1.0x10\^11VP) as intramuscular injection.

    Biological: AdCLD-CoV19

  • Experimental
    Group 4: selected dose

    Subject will receive single dose of AdCLD-CoV19 as intramuscular injection.

    Biological: AdCLD-CoV19

  • Experimental
    Group 5: selected dose

    Subject will receive single dose of AdCLD-CoV19 as intramuscular injection.

    Biological: AdCLD-CoV19

Interventions

  • BiologicalAdCLD-CoV19

    Replication-defective human adenovirus type 5/35 vector based vaccine expressing S protein of SARS-CoV-2.

06

What researchers measure

Primary outcomes

  1. Incidence of solicited adverse events(AEs)

    Time frame: Through 7 days post-vaccination

  2. Incidence of unsolicited AEs

    Time frame: Through 28, 56 days post-vaccination

Secondary outcomes

  1. Incidence of serious adverse events(SAEs)

    Time frame: Through 12 months post-vaccination

  2. Incidence of adverse events of special interest(AESIs)

    Time frame: Through 12 months post-vaccination

  3. Seroconversion rate(SCR) of neutralization antibody using wild type SARS-CoV-2

    Time frame: 4, 8 weeks post-vaccination

  4. Geometric mean titer(GMT) of neutralization antibody using wild type SARS-CoV-2

    Time frame: 4, 8 weeks post-vaccination

  5. GMT of S protein specific antibody

    Time frame: 2, 4, 8, 26, 52 weeks post-vaccination

  6. Index of T cell response

    Time frame: 2, 4, 26, 52 weeks post-vaccination

Other outcomes

  1. SCR of neutralization antibody using pseudovirus

    Time frame: 2, 4, 8, 26, 52 weeks post-vaccination

  2. GMT of neutralization antibody using pseudovirus

    Time frame: 2, 4, 8, 26, 52 weeks post-vaccination

  3. GMT of S protein receptor binding domain(RBD) specific antibody

    Time frame: 2, 4, 8, 26, 52 weeks post-vaccination

07

Study locations

5 sites
  • Korea University Ansan Hospital
    Ansan, Province, Korea, Republic of
  • The Catholic University of Korea, ST. Vincent's Hospital
    Suwon, Province, Korea, Republic of
  • Hallym University Kangnam Sacred Heart Hospital
    Seoul, State, Korea, Republic of
  • The Catholic University of Korea, Seoul ST. Mary's Hospital
    Seoul, State, Korea, Republic of
  • Korea University Guro Hospital
    Seoul, Korea, Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 28, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04666012
Lead sponsor
Cellid Co., Ltd.
Responsible party
Sponsor
First posted
Dec 14, 2020
Start date
Dec 29, 2020
Primary completion
Jul 9, 2021
Completion
Mar 27, 2023
Last update
Jul 28, 2023

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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